Synthesis of functional fluorinated polyhedral oligomeric silsesquioxane (“F-POSS”)

ABSTRACT

A method of forming a hydrophobic and oleophobic surface. The method including spin coating an F-POSS with 3,3-dichloro-1,1,1,2,2,-pentafluoropropane/1,3-dichloro-1,1,2,2,3-pentafluoropropane onto an inert surface. The F-POSS has a structure: 
     
       
         
         
             
             
         
       
     
     Each R f  represents a nonreactive, fluorinated organic group, R 1  represents a first monovalent organic group comprising at least two carbon atoms, and R 2  represents hydrogen or a second monovalent organic group comprising at least two carbon atoms. The F-POSS with 3,3-dichloro-1,1,1,2,2,-pentafluoropropane/1,3-dichloro-1,1,2,2,3-pentafluoropropane are then dried on the inert surface.

Pursuant to 37 C.F.R. § 1.78(a)(4), this application is a divisional ofpending U.S. application Ser. No. 15/708,382 (filed Sep. 19, 2017),which was a divisional of U.S. application Ser. No. 14/990,973 (filedJan. 8, 2016 and now U.S. Pat. No. 9,790,377), entitled SYNTHESIS OFFUNCTIONAL FLUORINATED POLYHEDRAL OLIGOMERIC SILSESQUIOXANE (“F-POSS”),which was a divisional of U.S. application Ser. No. 13/624,151 (filedSep. 21, 2012 and now U.S. Pat. No. 9,249,313), entitled SYNTHESIS OFFUNCTIONAL FLUORINATED POLYHEDRAL OLIGOMERIC SILSESQUIOXANE (F-POSS),which claimed the benefit of and priority to prior filed ProvisionalApplication Ser. No. 61/537,122, filed Sep. 21, 2011. This applicationis related to U.S. application Ser. No. 14/662,305 (AFD-1207DIV) filedMar. 19, 2015; Ser. No. 13/624,355 (AFD-1207) filed on Sep. 21, 2012;and 61/537,125 (AFD-1207P) filed Sep. 21, 2011. The disclosures of theseapplications are expressly incorporated herein by reference, in theirentireties.

RIGHTS OF THE GOVERNMENT

The invention described herein may be manufactured and used by or forthe Government of the United States for all governmental purposeswithout the payment of any royalty.

FIELD OF THE INVENTION

The present invention relates generally to silsesquioxane materials and,more particularly to silsesquioxane materials having increasedhydrophobicity.

BACKGROUND OF THE INVENTION

Polyhedral Oligomeric SilSesquioxanes (“POSS”) are cage-structureshaving a silicon-oxide (SiO_(1.5)) core surrounded by aliphatic oraromatic organic functionality. One such POSS derivative,octakis(1H,1H,2H,2H-heptadecafluorodecyl) POSS (“F-POSS”), possesses aperiphery of long-chain fluorinated alkyl groups and has been determinedto possess the lowest surface energy value of any crystalline solid(γ_(sv)=9.3 mN/m). Superhydrophobic (contact angles of a water dropletexceeding 150°) and oleophobic (repelled by oil) surfaces have beenproduced by casting F-POSS materials onto a substrate or blending theF-POSS material into a polymer matrix.

Conventionally, F-POSS has been used as standalone compounds withoutfurther reactive chemical functionality; however, this absence ofreactive chemical functionality limits solubility in common solvents,the mechanical robustness, and abrasion resistance of surfacescomprising these materials. One attempt to overcome such limitations hasbeen an incompletely-condensed F-POSS compound with silanolfunctionality, which enabled new, robust, low surface energy hybridmaterials. In fact, incompletely-condensed silsesquioxane frameworkshave emerged with alkyl and/or aryl peripheries and are operable assynthons for creating hybrid inorganic-organic materials, as models forsilica, for catalyst support, and as precursors for other silsesquioxanecontaining polymers.

Unfortunately, none of the conventional synthesis strategies are viableto produce long-chain (more than three carbon atoms) F-POSS compoundspossessing additional reactive or nonreactive functionality beyond alkylor aryl peripheries. Exemplary strategies, such as those described inU.S. Pat. No. 7,053,167, entitled SILSESQUIOXANE DERIVATIVE HAVINGFUNCTIONAL GROUP, issued to Ito et al. on Apr. 8, 2004 and U.S. Pat. No.7,291,747, entitled NOVEL SILICON COMPOUNDS AND PROCESS FOR PREPARATIONTHEREOF, issued to Oikawa et al. on Nov. 6, 2007 (disclosuresincorporated herein by reference, in their entireties), have notproduced long-chain F-POSS-(ONa)₃ having more than three carbon atoms.Modified methods have produced (3,3,3-trifluoropropyl)₇Si₇O₉(ONa)₃,which can be derivatized with long-chain fluorinated trichlorosilanes toproduce low surface energy materials, but the trifluoropropyl groups arestill limited in chain length.

While these conventional methods have proven successful for thesynthesis of incompletely-condensed compounds possessing alkyl- andaryl-functionality, there remains a need for a method of synthesizing anincompletely-condensed, long-chain F-POSS compound.

SUMMARY OF THE INVENTION

The present invention overcomes the foregoing problems and othershortcomings, drawbacks, and challenges of synthesizing anincompletely-condensed, long-chain F-POSS compound. While the inventionwill be described in connection with certain embodiments, it will beunderstood that the invention is not limited to these embodiments. Tothe contrary, this invention includes all alternatives, modifications,and equivalents as may be included within the spirit and scope of thepresent invention.

A method of forming a hydrophobic and oleophobic surface by spin coatingan F-POSS with3,3-dichloro-1,1,1,2,2,-pentafluoropropane/1,3-dichloro-1,1,2,2,3-pentafluoropropaneonto an inert surface. The F-POSS has a structure:

Each R_(f) represents a nonreactive, fluorinated organic group, R₁represents a first monovalent organic group comprising at least twocarbon atoms, and R₂ represents hydrogen or a second monovalent organicgroup comprising at least two carbon atoms. The F-POSS with3,3-dichloro-1,1,1,2,2,-pentafluoropropane/1,3-dichloro-1,1,2,2,3-pentafluoropropaneare then dried on the inert surface.

Still other embodiments of the present invention include method offorming a hydrophobic and oleophobic surface by spin coating an F-POSSwith3,3-dichloro-1,1,1,2,2,-pentafluoropropane/1,3-dichloro-1,1,2,2,3-pentafluoropropaneonto an inert surface. The F-POSS has a structure:

Each R_(f) represents a nonreactive, fluorinated organic group, R₁represents a first monovalent organic group comprising at least twocarbon atoms, and R₂ represents hydrogen or a second monovalent organicgroup comprising at least two carbon atoms. The F-POSS3,3-dichloro-1,1,1,2,2,-pentafluoropropane/1,3-dichloro-1,1,2,2,3-pentafluoropropaneare then dried on the inert surface.

One embodiment of the present invention is directed to a method ofinclude method of forming a hydrophobic and oleophobic surface by spincoating an F-POSS with3,3-dichloro-1,1,1,2,2,-pentafluoropropane/1,3-dichloro-1,1,2,2,3-pentafluoropropaneonto an inert surface. The F-POSS has a structure:

Each R_(f) represents a nonreactive, fluorinated organic group, R₁represents a first monovalent organic group comprising at least twocarbon atoms, and R₂ represents hydrogen or a second monovalent organicgroup comprising at least two carbon atoms. The F-POSS3,3-dichloro-1,1,1,2,2,-pentafluoropropane/1,3-dichloro-1,1,2,2,3-pentafluoropropaneare then dried on the inert surface.

The above and other objects and advantages of the present inventionshall be made apparent from the accompanying drawings and thedescriptions thereof.

BRIEF DESCRIPTION OF THE DRAWINGS

The accompanying drawings, which are incorporated in and constitute apart of this specification, illustrate embodiments of the presentinvention and, together with a general description of the inventiongiven above, and the detailed description of the embodiments givenbelow, serve to explain the principles of the present invention.

FIG. 1 is a schematic representation of the synthesis of one embodimentof an incompletely-condensed fluoroalkyl silsesquioxane.

FIG. 2 is a flow chart illustrating a method of synthesizing anincompletely-condensed fluoroalkyl silsesquioxane in accordance with oneembodiment of the present invention.

FIGS. 3A and 3B are schematic representations of two intermediates inthe synthesis of FIG. 1.

FIG. 4 is a schematic representation of a crystal structure determinedfor the incompletely-condensed fluoroalkyl silsesquioxane.

FIG. 5 is a schematic representation of a portion of the crystalstructure of FIG. 4, showing the intermolecular hydrogen bonding.

FIG. 6 is a schematic representation of crystal packing of a pluralityof incompletely-condensed fluoroalkyl silsesquioxane, illustrating thehydrogen bonds between silanols.

FIG. 7 is a schematic representation of the synthesis of one embodimentof a functionalized F-POSS compound.

DETAILED DESCRIPTION OF THE INVENTION

Turning now to the figures, and in particular to FIGS. 1 and 2, amulti-step synthetic method for converting a closed-cage F-POSS compound10 to an incompletely-condensed silsesquioxane compound 12 (hereafter,“disilanol F-POSS” 12), ((R_(f))₈Si₈O₁₁(OH)₂) is shown and described indetail. While not necessary, but for purposes of illustration, theF-POSS compound 10 includes nonfunctional groups, R_(f), which maycomprise —CH₂CH₂(CF₂)₇(CF₃); however, other moieties, may also beincluded. Indeed, not all R_(f) groups are required to have the samefunctionality.

More particularly, and as provided in the flow chart 14 of FIG. 2, asingle edge of the closed-cage F-POSS compound is opened (Block 16) withtrifluoromethane sulfonic acid, such as triflic acid (“TfOH”), in C₆F₆and CF₃SO₃H at 25° C. for 75 min. to form a first, unstableintermediate, which is illustrated herein as ditriflate POSS cage 18,((R_(f))₈Si₈O₁₁(OTf)₂), which is shown in FIG. 3A. Presence of theditriflate POSS cage formation was confirmed, despite spectralcomplexity, via ²⁹Si NMR. The spectrum demonstrated an equilibriumbetween the open and closed-cage silsesquioxane frameworks 10, 18, withresonances at −62.6 ppm, −65.0 ppm, and −67.7 ppm and an integratedratio of 2:2:4. While not wishing to be bound by theory, it is thoughtthat the inability to isolate the first intermediate, ditriflate POSS18, may be attributed to the strong electron-withdrawing effects of thefluorinated alkyl groups, R_(f).

The open, single end of the ditriflate compound 18 may then be bridgedwith a sulfate group 20 to a second, unstable intermediate, a bridgedsulfate compound 22 (FIG. 3B), ((R_(f))₈Si₈O₁₃(SO₂)), in Block 24 over areaction time, for example, of approximately 30 min., with an excess ofNBut₄HSO₄, under nitrogen. The reaction mixture separates into twoliquid layers: a first, yellow aqueous layer and a second, colorlessfluorinated solvent layer containing both of the closed-cage F-POSScompound 10 (FIG. 1) and the bridged sulfate compound 22. While thebridging sulfate moiety 20 appears to stabilize the electron-withdrawingF-POSS cage framework, the bridged sulfate compound 22 cannot beisolated. Its presence is confirmed, however, as another NMR-observedintermediate with ²⁹Si resonances at −64.5 ppm, −65.7 ppm, and −67.3 ppmwith an integrated ratio of 2:2:4. Although the bridged sulfate compound22 was not isolated, its endohedral geometry was deduced from x-raycrystallography data, described in detail below.

Referring again to FIG. 2, a polar fluorinated solvent/water mixture(for, example, a 10:1 ratio of solvent to water) is added to thefluorinated solvent layer (the colorless, aqueous layer above) of thereaction mixture for a time ranging from about 6 hours to about 12 hoursto convert the bridged sulfate compound 22 to the disilanol F-POSS 12 ofFIG. 1 (Block 26). Because the reaction requires water to be misciblewith the fluorinated solvent, the polar fluorinated solvent/watermixture is necessary to yield the desired, disilanol compound.

To isolate the disilanol F-POSS 12, ethyl acetate is added to thereaction mixture, and subsequently filtered. The filtrate is collected,concentrated, suspended again in chloroform, and filtered. The collectedfiltrand is dried under vacuum (about 18 hours at 50° C.) to yield theproduct with an overall yield of approximately 53% and a molecularweight of 4009 g/mol.

The principle side product of the conversion (Block 26) is the closedcage F-POSS compound 10. Due to subtle differences in solubility betweenthe closed cage F-POSS 10 and the disilanol F-POSS 12, disilanol F-POSS12 may be purified from the closed cage F-POSS 10, the latter of whichmay be subsequently recycled (Block 28). In accordance with oneembodiment of the present invention, the closed cage F-POSS 10 may beprecipitated from the reacted polar fluorinated solvent/water mixturewhile the disilanol F-POSS 12 is subsequently precipitated from a CHCl₃solution.

The structure of disilanol F-POSS 12 was determined by combustionanalysis and multinuclear NMR (¹H, ¹³C, ¹⁹F, and ²⁹Si). The ²⁹Si NMRspectrum displayed peaks at −59.0 ppm, −65.5 ppm, and −68.1 ppm, with anintegration ratio of 2:2:4, which are attributed to the C_(2v) symmetryof silsesquioxane. The peak at −59.0 ppm is attributed to the silanolgroups of the POSS framework.

The crystal structure 30 for disilanol F-POSS 12, shown in FIG. 4, wasobtained by growing crystals from slow evaporation in hexafluorobenzeneand using a 3-circle SMARTAPEX CCD (Kusing Bruker, Billerica, Mass.)with c-axis fixed at 54.748 and temperature of about 100 K with SMART V5.625 program. Graphite monochromated Cu_(Kα) (λ=1.54179 Å) radiationwas used for data collection, the SAINT V 6.22 program (Bruker, Corp.)was used for correcting Lorentz and polarization effects, and the SADABSprogram (Bruker, Corp.) was used for reflection scaling.

The structure was solved from C₆F₆ by direct methods (SHELXL-97, Bruker,Corp.) and all non-hydrogen atoms refined anisotropically usingfull-matrix, least squares refinement on F² and determined to bemonoclinic P2(1)/c. The structure contains rigid, helical-likefluoroalkyl chains that are similar to the closed cage F-POSS 10(FIG. 1) but are attached to the open Si—O frame-work by methylenegroups. The crystal structure supports the 2:2:4 ratio of silicon atomsas determined by ²⁹Si NMR spectroscopy of silicon atoms.

The crystal packing of two disilanol F-POSS molecules (illustrated as 12a and 12 b in FIG. 5, specifically, and in FIG. 6, generally, as crystalpacking) reveals a dimeric structure with two F-POSS cages formingintermolecular hydrogen bonds 32 a, 32 b between silanol groups on ofadjacent ones of the F-POSS cages 12 a, 12 b. This induces an increasein the lattice volume (approximately 12884 Å³) for disilanol F-POSS 12as compared to the volume of the closed cage F-POSS 10, which wasapproximately 6340 Å³. Like the hydrogen bonding between silanols onincompletely-condensed alkyl based POSS triols and diols, a dimericcontact is established from intermolecular disilanol compounds at adistance, d, of approximately 2.798 Å. These intermolecular silanols areslightly closer than intramolecular silanols, (illustrated on FIG. 5 asO1, O2, O3, O4, O5, O6, O7, O8, O9, O10, O11, O12, and O13), which areseparated by a distance of approximately 2.810 Å. As described in detailbelow, the intermolecular silanols are reactive to chlorosilanes.

To achieve an effective convergence on the structure, certain restrainswere applied, including, for example, as the thermal behavior of thestructure (SIMU and DELU commands for Si1 to F36C); ISOR was applied tofluorine atoms due to the associated disorder, intermolecular distances(C—C and C—F) were retrained using the SAME command. After a stableminimum was achieved, hydrogen atoms were added at calculated positionsto the alpha and beta carbon atoms. Hydrogen atoms on O1 and O13 wereadded using DFIX to restrain the distances (0.84 Å) to the respectiveoxygen atoms.

Additional details with respect to the crystal structure may be obtainedfrom the Cambridge Crystallographic Data Centre, available athttp://www.ccdc.com.ac.uk, Deposition Number 843485, the disclosure ofwhich is incorporated herein by reference, in its entirety.

Referring now to FIGS. 1, 2, and 6, disilanol F-POSS 12 is shown toreadily react with functional dichlorosilanes (Cl₂SiR₁R₂) to add aparticular or desired functionality (Block 34), which may include, forexample, superhydrophobic or oleophobic properties. According to oneembodiment of the present invention, the disilanol F-POSS 12 wascondensed with bis(n-octyl)dichlorosilane in the presence oftriethylamine to yield a functionalized F-POSS compound 36(approximately 46% yield), shown in FIG. 7, with a loss of HCl. Moreparticularly, bis(n-octyl)dichlorosilane and disilanol F-POSS 12, inC₆F₆, are mixed for 20 minutes and followed with the addition oftriethylamine, in C₆F₆, and further mixing for about 12 hours. Thesolution is filtered and poured into ethyl acetate, causing white solidprecipitate formation. Precipitate was removed via vacuum filtration,concentrated, dissolved in diethyl ether, and filtered again. Thefiltrate is then collected and cooled to 0° C., affording a whiteprecipitate, which is collected and dried under vacuum to a whitepowder. The primary side product isolated during the reaction was,again, the closed cage F-POSS 10 (FIG. 1).

Evaluation of the structure of the functionalized F-POSS compound 36included multinuclear NMR (¹H, ¹³C, ¹⁹F, and ²⁹Si), FT-IR, andcombustion analysis. NMR spectra were obtained on 300 MHz and 400 MHzspectrometers (Bruker Corp.) using 5 mm o.d. tubes. An inverse gated 30°pulse with a 12 second delay was used to acquire the ²⁹Si NMR spectra.The NMR spectrum produced ²⁹Si resonances at −17.8 ppm, −65.4 ppm, −68.2ppm, and −69.0 ppm, with a ratio of 1:2:4:2, of which the resonance at−17.8 ppm was attributed to dioctyl-functionalized Si atom. Large C—Hstretches observed at 2974 cm⁻¹ and 2871 cm⁻¹ in the FT-IR spectrum(Perkin Elmer Spectrum BX; Waltham, Mass.) supported the presence of thehydrocarbon chains, R₁, R₂.

As described herein, incompletely-condensed disilanol F-POSS compoundsmay be synthesized from fully condensed F-POSS compounds via athree-step reaction process and are reactive toward dichlorosilanes toproduce a functional F-POSS compound. Crystal structures demonstratesilanol groups are hydrogen bonded via intermolecular interaction, whichlowers the surface energy value beyond values observed with alkyl oraryl F-POSS compounds. Accordingly, the novel, tunable structure of thefunctionalized F-POSS compounds described herein provides unprecedentedaccess to fluorinated building blocks for manufacturing low surfaceenergy materials that are mechanically robust and abrasion resistant.For example, functionalized F-POSS 36 may be cast onto a substrate orblended with copolymers to produce surfaces having robust, abrasionresistant, superhydrophobic, and oleophobic material properties.

The following examples and comparative example illustrate particularproperties and advantages of some of the embodiments of the presentinvention. Furthermore, these are examples of reduction to practice ofthe present invention and confirmation that the principles described inthe present invention are therefore valid but should not be construed asin any way limiting the scope of the invention.

Example 1

Seven, long-chain F-POSS compounds, each having a different functionalgroup, were prepared in accordance with embodiments of the presentinvention. The F-POSS compounds included F-POSS (no additionalfunctional group), dihydroxy silyl F-POSS (Si—(OH)₂), dioctyl silylF-POSS (Si—((CH₂)₇CH₃)₂), dihexyl silyl F-POSS (Si—(C₆H₅)₂), vinylmethylsilyl F-POSS (Si—(CH₃)(CH═CH₂)), acrylate methylsilyl F-POSS(Si—((CH₃((CH₂)₃OC(O)CCH═CH₂)), and methylacrylate methylsilyl F-POSS(Si—(CH₃)((CH₂)₃OC(O)C(CH₃)═CH₂)). The synthesis of each compound wasconfirmed using combustion analysis, FT-IR, and multinuclear NMRspectroscopy.

The long-chain fluoroalkyl periphery on F-POSS results in desirable lowsurface energy characteristics. Interestingly, once a non-fluorinatedsegment was added to an edge of F-POSS, the solubility properties changedramatically. For example, the long hydrocarbon chains present indioctyl silyl F-POSS expanded solubility from just fluorinated solventsto include non-fluorinated solvents, such as Et₂O and CHCl₃. Even smallorganic modifications, such as the acrylate and methacrylate moieties onacrylate methylsilyl F-POSS and methylacrylate methylsilyl F-POSS,respectively, were sufficient to expand solubility to nonfluorinatedsolvents, such as Et₂O. However, phenyl and vinyl groups of dihexylsilyl F-POSS and vinyl methylsilyl F-POSS, respectively, did not improvethe solubility in non-fluorinated solvents, which may be attributed tothe rigidity of the phenyl and vinyl groups.

Films of each of the seven F-POSS compounds were spin cast onto sevenwafers (1 inch silicon) from solutions of Asahiklin-255(3,3-dichloro-1,1,1,2,2,-penta-fluoropropane/1,3-dichloro-1,1,2,2,3-pentafluoropropane)(10 mg/mL) at a rate of 900 rpm for 30 seconds and in accordance withthe methods described in S. S. CHHATRE et al. “FluoroalkylatedSilicon-Containing Surfaces—Estimation of Solid-Surface Energy,” ACSAppl. Mater. Interfaces. Vol. 2 (2010) 3544-3554, the disclosure ofwhich is incorporated herein by reference, in its entirety. Dihydroxysilyl F-POSS was spin cast in a similar manner but from C₆F₆ solution ata rate of 1400 rpm. Surfaces were smoothed to less than 5 nm rmsroughness to minimize any influence of surface roughness and topology asmeasured via atomic force microscopy using a Nanoscope IV (DigitalInstruments, Inc., whole-owned subsidiary of Veeco Instruments, Inc.,Plainview, N.Y.) and optical profilometry using a Wyko NT930 (VeecoInstruments, Inc.).

The influence of functionality on non-wetting behavior was determined byexamining static and dynamic contact angles of water and hexadecane oneach F-POSS film surface. Water and hexadecane 10 μL droplets werepositioned on the prepared wafers. Dynamic contact angles weredetermined by placing a 3 μL drop of the probing liquid onto a testsubstrate of a DataPhysics OCA20 goniometer (DataPhysics InstrumentsGmbH, Filderstadt, Germany). An additional 2 μL of the probing liquidwas added through a dispending needle at a rate of 0.2 μL/sec and then 3μL removed at 0.2 μL/sec. Video (ranging from 20 frames to 100 frames)was captured during the addition and removal of the probing liquid suchthat advancement and recession of a contact line between the droplet andthe test substrate, respectively, was observed and used for determiningthe advancing and receding contact angles, respectively. Measurementswere made from a “tangent lean” fit using a droplet fitting software(DataPhysics Instruments GmbH).

The open-cage framework of compound dihydroxy silyl F-POSS did notdisplay any adverse effect on the wetting behavior, which was attributedto the dimeric structure formed with silanols shielded from the surfaceof the film. A slight increase in contact angle hysteresis,θ_(rec)−θ_(adv), for dioctyl silyl F-POSS, vinyl methylsilyl F-POSS,acrylate methylsilyl F-POSS, and methylacrylate methylsilyl F-POSS wasobserved when wetted with water. This slight increase was not observedfor surfaces comprising the same films when wetted with hexadecane,except for dioctyl silyl F-POSS. The structure of dioctyl silyl F-POSScontains long aliphatic chains that potentially favor interaction with along-chain organic solvent, such as hexadecane.

Dihydroxy silyl F-POSS and dihexyl silyl F-POSS displayed the lowesthexadecane hysteresis values of all film surfaces and possessed slidingangles of approximately 7°. These initial measurements demonstrate thatmodifications of the F-POSS structure were found to be influential onwetting properties, either increasing or decreasing contact anglehysteresis.

TABLE 1 WATER HEXADECANE LONG-CHAIN F-POSS (θ_(adv), degrees) (θ_(rec),degrees) (θ_(adv), degrees) (θ_(rec), degrees) F-POSS 124.0 ± 0.5 109.6± 0.7 79.1 ± 0.4 65.1 ± 0.5 Dihydroxy silyl F-POSS 116.8 ± 0.4 111.0 ±0.6 77.4 ± 0.4 74.4 ± 0.8 Dioctyl silyl F-POSS 117.9 ± 0.5  95.5 ± 0.469.1 ± 1.2 23.1 ± 1.2 Dihexyl silyl F-POSS 116.2 ± 0.4 110.5 ± 0.5 76.0± 0.8 73.2 ± 0.4 Vinyl methylsilyl F-POSS 116.2 ± 0.4 100.6 ± 0.8 78.4 ±0.3 70.6 ± 2.3 Acrylate methylsilyl F-POSS 118.2 ± 1.0  90.6 ± 1.0 76.8± 0.3 67.8 ± 1.0 Methylacrylate methylsilyl F-POSS 117.0 ± 0.6  93.8 ±1.5 78.1 ± 0.4 63.0 ± 1.2

While the present invention has been illustrated by a description ofvarious embodiments, and while these embodiments have been described insome detail, they are not intended to restrict or in any way limit thescope of the appended claims to such detail. Additional advantages andmodifications will readily appear to those skilled in the art. Thevarious features of the invention may be used alone or in anycombination depending on the needs and preferences of the user. This hasbeen a description of the present invention, along with methods ofpracticing the present invention as currently known. However, theinvention itself should only be defined by the appended claims.

What is claimed is:
 1. A hydrophobic and oleophobic substrate surfacecomprising: a substrate having a surface; and a hydrophobic andoleophobic layer on the surface of the substrate, the hydrophobic andoleophobic layer comprising an F-POSS with3,3-dichloro-1,1,1,2,2-pentafluoropropane/1,3-dichloro-1,1,2,2,3-pentafluoropropaneonto an inert surface, the F-POSS having a structure:

where each R_(f) represents a nonreactive, fluorinated organic group, R₁represents a first monovalent organic group comprising at least twocarbon atoms and is selected from the group consisting of —(CH₂)₇CH₃,—(CH₂)₃OC(O)CH═CH₂, and —(CH₂)₃OC(O)C(CH₃)═CH₂, and R₂ representshydrogen or a second monovalent organic group comprising at least twocarbon atoms.
 2. The hydrophobic and oleophobic substrate surface ofclaim 1, wherein R_(f) represents —CH₂CH₂(CF₂)₇CF₃.
 3. The hydrophobicand oleophobic substrate surface of claim 1, wherein the firstmonovalent organic group, the second monovalent organic group, or bothcomprises at least three carbon atoms.
 4. The hydrophobic and oleophobicsubstrate surface of claim 1, wherein R_(f) represents a fluorinatedalkyl group.
 5. The hydrophobic and oleophobic substrate surface ofclaim 1, wherein each R_(f) is separately selected from the groupconsisting of fluorotetradecyl, fluorododecyl, fluorodecyl, fluorooctyl,fluorohexyl, and hexafluoro-i-butyl.